Chiral synthetic pseudopeptidic derivatives as triplet excited state quenchers-Reference-Cited by-同舟云学术

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Chiral synthetic pseudopeptidic derivatives as triplet excited state quenchers

Published:2009-08 Issue:34 Volume:50 Page:4859-4862
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Salom-Roig Xavier J.,Martínez Jean,Burguete M. Isabel,Galindo Francisco,Luis Santiago V.,Miranda Miguel A.,Morant-Miñana María C.,Pérez-Prieto Julia

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Peptides as protein binding site mimetics

2. β-Hairpin Peptidomimetics: Design, Structures and Biological Activities

3. Stereodifferentiation in the Decay of Triplets and Biradicals Involved in Intramolecular Hydrogen Transfer from Phenols or Indoles to π,π* Aromatic Ketones

4. Regio- and stereo-selectivity in the intramolecular quenching of the excited benzoylthiophene chromophore by tryptophan

5. Enantioselective Discrimination in the Intramolecular Quenching of an Excited Aromatic Ketone by a Ground-State Phenol

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Efficient monoacylation of symmetrical secondary alkanediamines and synthesis of unsymmetrical diacylated alkanediamines. A new L-proline-based organocatalyst;Arkivoc;2020-01-12

2. Triplet Excited State Behavior of Naphthalene-Based Pseudopeptides in the Presence of Energy Donors;The Journal of Physical Chemistry B;2012-08-10

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